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Horizontal scalp biopsy sections are better for diagnosing alopecia areata, showing fewer hair follicles and more miniaturized hairs.

Early medical support for transgender youth is important for their health, with low regret for gender-affirming hormone use and a need for knowledgeable care providers.

Fluridil safely promotes hair growth in men with androgenetic alopecia.

Lichen Planopilaris in teens is rare, often misdiagnosed, and responds well to steroids.

Trichotillomania, a disorder where people compulsively pull out their own hair, often starts around age 12, is more common in adult females, and can be treated with behavior therapy and medication.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Pediatric dermatologists need to understand the unique skin health needs of LGBTQIA youth to provide better care.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

Woman's hair loss diagnosis changed from CTE to AA; multiple biopsies important for accurate diagnosis.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

P-selectin is not the only factor that prevents scarring in fetal wound healing in mice.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

To improve use of the contraceptive DMPA among adolescents, effectively manage side effects like menstrual changes and weight gain through counseling and guidance.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Diagnosing and managing PCOS in teens is hard, but early diagnosis and lifestyle changes are key, and more research is needed for long-term health.

Fluridil promotes hair growth safely and effectively for androgenetic alopecia.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The study suggests that complement activation, not immunoglobulins, may be important in erythema nodosum leprosum.

Eating more protein during fast weight loss can prevent hair loss.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

Malnutrition can cause unusual eyelash growth and hair loss.

The document recommends a team-based approach and personalized care for managing diabetes in teenagers.

Spironolactone may help treat excessive hair growth in girls, but more research is needed.

Two children grew extra hair from taking omeprazole, which went away after they stopped the medication.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.